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a) b - École Polytechnique de Montréal

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with a polyelectrolyte(Jaffar et al., 2004). In the LbL approach, the adsorption process involves<br />

consecutive and alternate <strong>de</strong>position of polyelectrolytes including polyanions and polycations<br />

driven by electrostatic forces, or other interactions such as hydrogen bonding. Although<br />

oppositely charged polyelectrolyte si<strong>de</strong> groups represent a quite powerful attraction, some other<br />

types of intermolecular interactions between polyelectrolytes such as van –<strong>de</strong>r Waals, dipole-<br />

dipole, and ion-dipole, involve chains of polyelectrolyte and molecules of solvent.<br />

Polyelectrolytes or polysalts are similar to both high molecular weight compounds (polymers)<br />

and electrolytes (salts). This means that due to electrolyte groups, they are electrically<br />

conductive in aqueous solutions and because of macromolecules, their solutions are viscous. In<br />

the LbL technique, each step involves dipping of the substrate into an oppositely-charged<br />

solution followed by a rinsing step with water. To maintain film growth until the <strong>de</strong>sired<br />

thickness or number of bilayers is achieved, alternate dipping is repeated. A stepwise increase of<br />

multilayer thickness or film mass with each <strong>de</strong>position step is expected. Thickness of each<br />

monolayer in this method is dictated by the polymer geometry; also supramolecular structures of<br />

alternately charged polymers can be controlled by polymer combination, surface charges, and<br />

solution parameters(Decher, 1997). The thickness increment after each <strong>de</strong>position, referred to as<br />

growth rate, shows a steady state regime of multilayer assembly with several nanometers<br />

thickness for each layer.<br />

Decher(Decher & Schlenoff, 2003) mentioned two significant advantages for layer-by-layer<br />

assembly method: 1) surface properties of existing objects and <strong>de</strong>vices can be controlled by<br />

controlling surface functionality, and 2) thin-film <strong>de</strong>vices can be fabricated in a very controlled<br />

way by template-assisted assembly. Properties of <strong>de</strong>vices can be engineered by controlling the<br />

spatial arrangement of functionality in multimaterial-layered nanocomposites. There are some<br />

more advantages for this technique in comparison with other methods such as its low-cost<br />

preparation and its environmentally friendliness. Kotov(Kotov, Dekany, & Fendler, 1995) ad<strong>de</strong>d<br />

that by varying the total number of <strong>de</strong>posited layers, the total thickness of the coating can be<br />

controlled with a precision of a few nanometers. Thus, the technique is exceptionally simple,<br />

precise, versatile and scale-up friendly.<br />

After showing the <strong>de</strong>position of oppositely charged polymer layers, the number of published<br />

papers on polyelectrolyte multilayer has grown exponentially. More than 200 published papers<br />

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